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Human Disease
hereditary spastic paraplegia 91
- Term ID
- DOID:0070643
- Synonyms
-
- autosomal dominant spastic paraplegia 91
- autosomal dominant spastic paraplegia 91 with or without cerebellar ataxia
- Definition
- A hereditary spastic paraplegia that has_material_basis_in heterozygous mutation in the SPTAN1 gene on chromosome 9q34. (2)
- References
- Ontology
- Human Disease ( DOID:0070643 )
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Genes Involved
Zebrafish Models